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18605-26-0

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18605-26-0 Usage

General Description

N-[(Phenylmethoxy)carbonyl]-beta-alanine tert-butyl ester is a chemical compound that belongs to the class of carboxylic acid derivatives. It is an ester derivative of beta-alanine, a naturally occurring beta-amino acid, and is also known as tert-butyl N-[(phenylmethoxy)carbonyl]beta-alaninate. N-[(Phenylmethoxy)carbonyl]-beta-alanine tert-butyl ester is mainly used in the field of pharmaceuticals and research as a building block in the synthesis of various pharmaceutical compounds. It has also been studied for its potential role in drug delivery systems and as a prodrug for improving the bioavailability of certain drugs. The chemical structure of this compound includes a phenylmethoxy carbonyl group attached to the beta-alanine backbone via an ester linkage, with a tert-butyl group providing stability to the molecule.

Check Digit Verification of cas no

The CAS Registry Mumber 18605-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,0 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18605-26:
(7*1)+(6*8)+(5*6)+(4*0)+(3*5)+(2*2)+(1*6)=110
110 % 10 = 0
So 18605-26-0 is a valid CAS Registry Number.

18605-26-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-(phenylmethoxycarbonylamino)propanoate

1.2 Other means of identification

Product number -
Other names N-Cbz-beta-alanine tert-butyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18605-26-0 SDS

18605-26-0Relevant articles and documents

Compound for targeted ubiquitination degradation of ERRalpha protein and pharmaceutical composition and application thereof

-

Paragraph 0234-0238, (2020/06/20)

The invention provides a compound with a structure shown as a formula (I), which has the effects of inhibiting ERRalpha protein activity and degrading ERRalpha protein activity, has relatively strongsubtype selectivity and can also effectively inhibit tri

Synthesis and self-association properties of flexible guanidiniocarbonylpyrrole-carboxylate zwitterions in DMSO: Intra- versus intermolecular ion pairing

Schmuck, Carsten,Rehm, Thomas,Geiger, Lars,Schaefer, Mathias

, p. 6162 - 6170 (2008/02/10)

(Chemical Equation Presented) We have synthesized a new class of flexible zwitterions 6a-e, in which a carboxylate is linked via an alkyl chain with variable length (one to five methylene groups) to a guanidiniocarbonylpyrrole cation. The self-association properties of these zwitterions were determined by NMR dilution studies in DMSO and by ESI-MS experiments. The stability and hence also the size of the aggregates formed via self-assembly is critically dependent on the length and therefore flexibility of the spacer. Whereas the smallest zwitterion 6a forms large aggregates already at low concentrations, the more flexible zwitterions only form small oligomers (6b) or dimers (6c-e) at much larger concentrations. The differences between the five zwitterions can be explained based on the different extent of intramolecular ion pairing within the monomers. Any intramolecular ion pairing, which becomes possible with increasing linker length, stabilizes the monomer and therefore destabilizes any oligomer.

The use of cellulose (chromatography paper) as a cheap, versatile and non-covalent support for organic molecules during multi-step synthesis

Shanahan, Stephen E.,Byrne, Douglas D.,Inglis, Graham G. A.,Alam, Mahbub,Macdonald, Simon J. F.

, p. 2554 - 2555 (2007/10/03)

Cellulose chromatography paper provides a novel non-covalent support for synthesis and in-situ purification of multi-dimensional arrays.

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